Clinical Trials
Clinical trials are systematic research studies conducted in human participants to evaluate the safety, efficacy, and effectiveness of medical interventions such as drugs, devices, treatments, or preventive measures. They follow rigorous scientific protocols to generate reliable data for regulatory approval and clinical practice. In software development, this involves designing and implementing systems to manage trial data, ensure compliance, and support analysis.
Developers should learn about clinical trials when building healthcare software, clinical research platforms, or data management systems for pharmaceutical and biotech industries. It's essential for roles involving electronic data capture (EDC) systems, regulatory compliance (e.g., FDA 21 CFR Part 11), and data analytics in life sciences. Understanding clinical trials ensures software meets ethical, legal, and scientific standards for patient safety and data integrity.